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myc ‐Immortalized Microglial Cells Express a Functional Platelet‐Activating Factor Receptor
Author(s) -
Righi Marco,
Letari Ornella,
Sacerdote Paola,
Marangoni Franca,
Miozzo Amelia,
Nicosia Simonetta
Publication year - 1995
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1046/j.1471-4159.1995.64010121.x
Subject(s) - microglia , microbiology and biotechnology , immortalised cell line , biology , platelet activating factor , cell culture , arachidonic acid , extracellular , neuroglia , calcium in biology , intracellular , inflammation , central nervous system , immunology , endocrinology , biochemistry , enzyme , genetics
The autacoid platelet‐activating factor (PAF) takes part in a complex network of interactions regarding the cellular components of nervous tissues. Efforts aimed at characterizing the effects of PAF in the brain have been recently focalized on neurons because PAF exerts pleiotropic effects on these cells. Less attention has instead been paid to the glial component of the brain. We have used microglial cell lines immortalized from 13‐day‐old mouse embryo brains by a myc ‐transducing retrovirus. When exposed to physiological doses of PAF, immortalized microglial cells showed increases in intracellular free calcium concentrations due to release of calcium from internal stores, as well as to extracellular calcium influxes. These profiles of reactivity were independent from the immortalizing process, being observable in primary microglial cultures and in immortalized clones showing different proliferative rates. PAF was also able to induce transient expression of the c‐ fos protooncogene in serum‐starved cultures and induced a strong chemotactic response in microglial cells. In contrast with control macrophage cultures, PAF did not promote prostaglandin or leukotriene synthesis in immortalized cells. This was most likely due to the low amount of total arachidonic acid found in immortal microglia, with respect to that observed in freshly isolated cells. Our data suggest that several of the effects observed after PAF stimulation might be independent from PAF‐induced arachidonic acid metabolism. The availability of an in vitro microglial model might now help in studying the proinflammatory effects of PAF, both direct or microglia mediated, in the neural environment.